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microsoft office edc ctms tmf ich-gcp📋 Description
- Serve as site liaison for study teams and ensure ICH-GCP compliance.
- Manage Investigator Site Files and coordinate with shipping vendors.
- Use CTMS to track milestones and site activities.
- Perform data review, query resolution, and TMF updates.
- Coordinate site communications, newsletters, and core documents.
- Assist site visits, payments, invoices, and mentor trainees.
🎯 Requirements
- Bachelor's degree or international equivalent.
- Minimum 2 years of relevant experience.
- MS Office proficiency (Outlook/Word/Excel/PowerPoint).
- English fluency, written and spoken.
- Working knowledge of the drug development process.
- Ability to travel as needed.
- Preferred: solid experience in clinical research.
🎁 Benefits
- Remote work environment.
- Equal Opportunity Employer.
- Disability accommodation available.
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